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rs200818962

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200818962(C;T)
Make rs200818962(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position31962494
GeneSKIV2L
is asnp
is mentioned by
dbSNPrs200818962
ebirs200818962
HLIrs200818962
Exacrs200818962
Varsomers200818962
Maprs200818962
PheGenIrs200818962
hapmaprs200818962
1000 genomesrs200818962
hgdprs200818962
ensemblrs200818962
gopubmedrs200818962
geneviewrs200818962
scholarrs200818962
googlers200818962
pharmgkbrs200818962
gwascentralrs200818962
openSNPrs200818962
23andMers200818962
23andMe allrs200818962
SNP Nexus

SNPshotrs200818962
SNPdbers200818962
MSV3drs200818962
GWAS Ctlgrs200818962
Max Magnitude0
ClinVar
Risk rs200818962(T;T)
Alt rs200818962(T;T)
Reference rs200818962(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SKIV2L
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.31930271C>T
CLNSRC
CLNACC RCV000224429.1,